Jonathan Mill

57.5k total citations · 7 hit papers
260 papers, 25.8k citations indexed

About

Jonathan Mill is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Jonathan Mill has authored 260 papers receiving a total of 25.8k indexed citations (citations by other indexed papers that have themselves been cited), including 173 papers in Molecular Biology, 108 papers in Genetics and 54 papers in Psychiatry and Mental health. Recurrent topics in Jonathan Mill's work include Epigenetics and DNA Methylation (149 papers), Genetic Syndromes and Imprinting (48 papers) and Genetics and Neurodevelopmental Disorders (45 papers). Jonathan Mill is often cited by papers focused on Epigenetics and DNA Methylation (149 papers), Genetic Syndromes and Imprinting (48 papers) and Genetics and Neurodevelopmental Disorders (45 papers). Jonathan Mill collaborates with scholars based in United Kingdom, United States and Canada. Jonathan Mill's co-authors include Ian Craig, Avshalom Caspi, Terrie E. Moffitt, Richie Poulton, Joseph L. McClay, Judy Martin, Leonard C. Schalkwyk, Karen Sugden, Antony W. Braithwaite and Alan Taylor and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Jonathan Mill

254 papers receiving 25.0k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Influence of Life Stress on Depression: Moderation by a Polymorphism in the 5-HTT Gene

2003 5.5k citations Avshalom Caspi, Karen Sugden et al. Science profile →
Role of Genotype in the Cycle of Violence in Maltreated Children

2002 2.8k citations Avshalom Caspi, Joseph L. McClay et al. Science profile →
Transcriptomic analysis of autistic brain reveals convergent molecular pathology

2011 1.3k citations Jonathan Mill, Daniel H. Geschwind et al. profile →
A data-driven approach to preprocessing Illumina 450K methylation array data

2013 671 citations Chloe C. Y. Wong, Katie Lunnon et al. profile →
Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis

2008 583 citations Jonathan Mill et al. profile →
TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration

2009 546 citations Jonathan Mill et al. profile →
Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood

2012 494 citations Katie Lunnon, Cristian Coarfa et al. Genome biology profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Jonathan Mill	10.2k	6.0k	5.5k	3.9k	3.7k	260	25.8k
Joel Gelernter	6.8k 0.7×	5.6k 0.9×	5.9k 1.1×	3.2k 0.8×	3.7k 1.0×	589	26.7k
Ian Craig	6.2k 0.6×	4.8k 0.8×	5.9k 1.1×	2.6k 0.7×	3.0k 0.8×	285	22.4k
Gustavo Turecki	8.8k 0.9×	3.4k 0.6×	11.6k 2.1×	2.9k 0.7×	5.7k 1.5×	587	33.2k
Patrick F. Sullivan	7.2k 0.7×	9.6k 1.6×	8.3k 1.5×	3.1k 0.8×	6.0k 1.6×	428	29.8k
Ole A. Andreassen	6.2k 0.6×	5.3k 0.9×	4.1k 0.7×	6.4k 1.6×	10.2k 2.8×	936	31.0k
Nancy L. Pedersen	5.0k 0.5×	5.6k 0.9×	5.4k 1.0×	2.7k 0.7×	6.0k 1.6×	652	37.5k
James L. Kennedy	6.2k 0.6×	4.6k 0.8×	5.8k 1.1×	5.0k 1.3×	9.1k 2.5×	678	26.7k
David Goldman	12.8k 1.2×	6.3k 1.1×	7.6k 1.4×	8.6k 2.2×	7.0k 1.9×	651	48.6k
Elisabeth B. Binder	5.9k 0.6×	2.2k 0.4×	5.1k 0.9×	1.8k 0.5×	1.7k 0.5×	331	22.7k
Marcella Rietschel	3.6k 0.4×	3.9k 0.7×	2.6k 0.5×	3.6k 0.9×	4.8k 1.3×	470	17.3k

Countries citing papers authored by Jonathan Mill

Since Specialization

Citations

This map shows the geographic impact of Jonathan Mill's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jonathan Mill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan Mill more than expected).

Fields of papers citing papers by Jonathan Mill

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jonathan Mill. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jonathan Mill. The network helps show where Jonathan Mill may publish in the future.

Co-authorship network of co-authors of Jonathan Mill

This figure shows the co-authorship network connecting the top 25 collaborators of Jonathan Mill. A scholar is included among the top collaborators of Jonathan Mill based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jonathan Mill. Jonathan Mill is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Walker, Emma, Emma Dempster, Barry A. Chioza, et al.. (2025). Guidance for the design and analysis of cell-type-specific DNA methylation epidemiology studies. Briefings in Bioinformatics. 26(4). 1 indexed citations

Clifton, Nicholas E., Emma Walker, Isabel Castanho, et al.. (2025). Setd1a Loss-of-function Disrupts Epigenetic Regulation of Ribosomal Genes via Altered DNA Methylation. Schizophrenia Bulletin. 52(2). 1 indexed citations

Namboori, Seema C., et al.. (2025). Rapid and inducible mislocalization of endogenous TDP43 in a novel human model of amyotrophic lateral sclerosis. eLife. 13. 2 indexed citations

Gillespie, Amy, Emma Walker, Eilís Hannon, et al.. (2024). Longitudinal changes in DNA methylation associated with clozapine use in treatment-resistant schizophrenia from two international cohorts. Translational Psychiatry. 14(1). 390–390. 3 indexed citations

Leung, Szi Kay, Rosemary A. Bamford, Aaron R. Jeffries, et al.. (2024). Long-read transcript sequencing identifies differential isoform expression in the entorhinal cortex in a transgenic model of tau pathology. Nature Communications. 15(1). 6458–6458. 5 indexed citations

Pishva, Ehsan, Arunima Roy, Gabriela Ortega, et al.. (2023). Genome‐wide DNA methylation analysis of aggressive behaviour: a longitudinal population‐based study. Journal of Child Psychology and Psychiatry. 64(7). 998–1006. 2 indexed citations

Caspi, Avshalom, Gemma Shireby, Jonathan Mill, et al.. (2023). Accelerated Pace of Aging in Schizophrenia: Five Case-Control Studies. Biological Psychiatry. 95(11). 1038–1047. 18 indexed citations

Shireby, Gemma, Yasuo Miki, Emmanuelle Viré, et al.. (2022). Epigenetic age acceleration is associated with oligodendrocyte proportions in MSA and control brain tissue. Neuropathology and Applied Neurobiology. 49(1). e12872–e12872. 9 indexed citations

Shireby, Gemma, Emma Dempster, Joe Burrage, et al.. (2022). Uncertainty quantification of reference-based cellular deconvolution algorithms. Epigenetics. 18(1). 2137659–2137659. 8 indexed citations

10.

Flynn, Robert J., Aaron R. Jeffries, Gemma Shireby, et al.. (2022). Evaluation of nanopore sequencing for epigenetic epidemiology: a comparison with DNA methylation microarrays. Human Molecular Genetics. 31(18). 3181–3190. 8 indexed citations

11.

Gunasekara, Chathura, Eilís Hannon, Harry A. Mackay, et al.. (2021). A machine learning case–control classifier for schizophrenia based on DNA methylation in blood. Translational Psychiatry. 11(1). 412–412. 14 indexed citations

12.

Leung, Szi Kay, Aaron R. Jeffries, Isabel Castanho, et al.. (2021). Full-length transcript sequencing of human and mouse cerebral cortex identifies widespread isoform diversity and alternative splicing. Cell Reports. 37(7). 110022–110022. 84 indexed citations

13.

Sugden, Karen, Eilís Hannon, Louise Arseneault, et al.. (2020). Patterns of Reliability: Assessing the Reproducibility and Integrity of DNA Methylation Measurement. Patterns. 1(2). 100014–100014. 81 indexed citations

14.

Wong, Chloe C. Y., Rebecca G. Smith, Eilís Hannon, et al.. (2019). Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue. Human Molecular Genetics. 28(13). 2201–2211. 59 indexed citations

15.

Kant, Immanuel, et al.. (2018). Realism and Idealism as Political Concepts. International Journal of Managerial Studies and Research. 6(11).

16.

Hannon, Eilís, Olivia Knox, Karen Sugden, et al.. (2018). Characterizing genetic and environmental influences on variable DNA methylation using monozygotic and dizygotic twins. PLoS Genetics. 14(8). e1007544–e1007544. 117 indexed citations

17.

O’Brien, Heath, Eilís Hannon, Matthew Hill, et al.. (2018). Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders. Genome biology. 19(1). 194–194. 84 indexed citations

18.

Smith, Adam R., Rebecca G. Smith, Eilís Hannon, et al.. (2016). Increased DNA methylation near TREM2 is consistently seen in the superior temporal gyrus in Alzheimer's disease brain. Neurobiology of Aging. 47. 35–40. 67 indexed citations

19.

Lunnon, Katie & Jonathan Mill. (2013). Epigenetic studies in Alzheimer's disease: Current findings, caveats, and considerations for future studies. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(8). 789–799. 59 indexed citations

20.

Caspi, Avshalom, Joseph L. McClay, Terrie E. Moffitt, et al.. (2002). Role of Genotype in the Cycle of Violence in Maltreated Children. Science. 297(5582). 851–854. 2791 indexed citations breakdown →

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact